Liu X - Search Results

1

[Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy].

Sun H, Zhang Y, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):121-7. doi: 10.3760/cma.j.issn.1003-9406.2009.02.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350499 Chinese.

2

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Lu J, Chen Y, Zhang Y, Pan H, Liu X, Jiang Y, Du W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Jun;19(3):183-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12048673 Chinese.

3

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Among authors: liu x. J Hum Genet. 2008;53(8):769-774. doi: 10.1007/s10038-008-0306-y. Epub 2008 Jun 20. J Hum Genet. 2008. PMID: 18566737

4

Gene symbol: SCN1A. Disease: Generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Among authors: liu x. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846618 No abstract available.

5

Gene symbol: GABRG2. Disease: Generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Among authors: liu x. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846619 No abstract available.

6

[Analysis of the GABRG2 gene mutation in a Chinese family with generalized epilepsy with febrile seizures plus].

Sun H, Zhang Y, Liu X, Ma X, Wu H, Xu K, Qi Y, Wu X. Sun H, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):611-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065515 Chinese.

7

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.

Sun H, Zhang Y, Liu X, Ma X, Yang Z, Qin J, Jiang Y, Qi Y, Wu X. Sun H, et al. Among authors: liu x. J Hum Genet. 2010 Jul;55(7):421-7. doi: 10.1038/jhg.2010.39. Epub 2010 Apr 30. J Hum Genet. 2010. PMID: 20431604

8

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Zhang X, Liu X, Wu X. Yang X, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):679-85. doi: 10.3760/cma.j.issn.1003-9406.2014.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449067 Chinese.

9

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

Yang X, Zhang Y, Xu X, Yu X, Zhang X, Yang Z, Wang S, Wu Y, Liu X, Wu X. Yang X, et al. Among authors: liu x. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):806-11. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582463 Chinese.

10

[Analysis of parental origin of de novo SCN1A mutations in Dravet syndrome].

Sun H, Zhang Y, Xu X, Liu X, Wu X. Sun H, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):457-61. doi: 10.3760/cma.j.issn.1003-9406.2015.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252084 Chinese.

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